Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model

Abstract Muscle loss is a debilitating side effect to prostate cancer (PCa) experienced by nearly 60% of men. The purpose of this study was to test the hypothesis that Nexrutine®, a bark extract from the Phellodendrum amurense, can protect against prostate cancer induced muscle loss in a similar man...

Full description

Bibliographic Details
Main Authors: Darpan I. Patel, Derek Wallace, Kira Abuchowski, Paul Rivas, Amber Gallegos, Nicolas Musi, Addanki Pratap. Kumar
Format: Article
Language:English
Published: Wiley 2019-08-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.14217
_version_ 1811224351162236928
author Darpan I. Patel
Derek Wallace
Kira Abuchowski
Paul Rivas
Amber Gallegos
Nicolas Musi
Addanki Pratap. Kumar
author_facet Darpan I. Patel
Derek Wallace
Kira Abuchowski
Paul Rivas
Amber Gallegos
Nicolas Musi
Addanki Pratap. Kumar
author_sort Darpan I. Patel
collection DOAJ
description Abstract Muscle loss is a debilitating side effect to prostate cancer (PCa) experienced by nearly 60% of men. The purpose of this study was to test the hypothesis that Nexrutine®, a bark extract from the Phellodendrum amurense, can protect against prostate cancer induced muscle loss in a similar manner as exercise, using the transgenic adenocarcinoma of mouse prostate (TRAMP) model. Forty‐five, 8‐ to 10‐week old TRAMP mice were randomized to either control, Nexrutine® (600 mg/kg pelleted in chow) or exercise (voluntary wheel running). Mice were serially sacrificed at weeks 4, 8, 12, and 20, at which time either the left or right gastrocnemius muscle was harvested, weighted, and frozen. Proteolysis inducing factor (PIF), ubiquitin, and NF‐κB concentrations were quantified using ELISA kits. Nexrutine® and exercise were equally able to protect TRAMP mice against PCa‐induced muscle loss (P = 0.04). Both interventions decreased intramuscular PIF concentrations at 20 weeks compared to control (P < 0.05). A treatment effect was also observed when all time points were combined with exercise significantly lowering PIF concentrations (P < 0.01). Exercise significantly lowered intramuscular ubiquitin concentrations in weeks 4, 8, and 20 compared to control mice (P < 0.001). A treatment effect was also observed with exercise significantly lowering ubiquitin compared to control mice (P < 0.001). No significant changes were observed for NF‐κB. The results of this investigation demonstrate that PCa‐induced muscle loss can be attenuated with the herbal supplement Nexrutine®. This investigation provides preliminary evidence to support continued research into Nexrutine® as a potential exercise analog in protecting against muscle loss.
first_indexed 2024-04-12T08:47:54Z
format Article
id doaj.art-00bf1b87b0fa4220a62981c7a6f3ecd8
institution Directory Open Access Journal
issn 2051-817X
language English
last_indexed 2024-04-12T08:47:54Z
publishDate 2019-08-01
publisher Wiley
record_format Article
series Physiological Reports
spelling doaj.art-00bf1b87b0fa4220a62981c7a6f3ecd82022-12-22T03:39:39ZengWileyPhysiological Reports2051-817X2019-08-01716n/an/a10.14814/phy2.14217Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse modelDarpan I. Patel0Derek Wallace1Kira Abuchowski2Paul Rivas3Amber Gallegos4Nicolas Musi5Addanki Pratap. Kumar6School of Nursing University of Texas Health Science Center at San Antonio San Antonio TexasSchool of Nursing University of Texas Health Science Center at San Antonio San Antonio TexasSchool of Nursing University of Texas Health Science Center at San Antonio San Antonio TexasDepartment of Urology, School of Medicine University of Texas Health Science Center at San Antonio San Antonio TexasSchool of Nursing University of Texas Health Science Center at San Antonio San Antonio TexasBarshop Institute for Aging University of Texas Health Science Center at San Antonio San Antonio TexasMays Cancer Center at UT Health San Antonio San Antonio TexasAbstract Muscle loss is a debilitating side effect to prostate cancer (PCa) experienced by nearly 60% of men. The purpose of this study was to test the hypothesis that Nexrutine®, a bark extract from the Phellodendrum amurense, can protect against prostate cancer induced muscle loss in a similar manner as exercise, using the transgenic adenocarcinoma of mouse prostate (TRAMP) model. Forty‐five, 8‐ to 10‐week old TRAMP mice were randomized to either control, Nexrutine® (600 mg/kg pelleted in chow) or exercise (voluntary wheel running). Mice were serially sacrificed at weeks 4, 8, 12, and 20, at which time either the left or right gastrocnemius muscle was harvested, weighted, and frozen. Proteolysis inducing factor (PIF), ubiquitin, and NF‐κB concentrations were quantified using ELISA kits. Nexrutine® and exercise were equally able to protect TRAMP mice against PCa‐induced muscle loss (P = 0.04). Both interventions decreased intramuscular PIF concentrations at 20 weeks compared to control (P < 0.05). A treatment effect was also observed when all time points were combined with exercise significantly lowering PIF concentrations (P < 0.01). Exercise significantly lowered intramuscular ubiquitin concentrations in weeks 4, 8, and 20 compared to control mice (P < 0.001). A treatment effect was also observed with exercise significantly lowering ubiquitin compared to control mice (P < 0.001). No significant changes were observed for NF‐κB. The results of this investigation demonstrate that PCa‐induced muscle loss can be attenuated with the herbal supplement Nexrutine®. This investigation provides preliminary evidence to support continued research into Nexrutine® as a potential exercise analog in protecting against muscle loss.https://doi.org/10.14814/phy2.14217atrophyinflammationnatural productneoplasm of the prostateproteolysis‐inducing factor
spellingShingle Darpan I. Patel
Derek Wallace
Kira Abuchowski
Paul Rivas
Amber Gallegos
Nicolas Musi
Addanki Pratap. Kumar
Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model
Physiological Reports
atrophy
inflammation
natural product
neoplasm of the prostate
proteolysis‐inducing factor
title Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model
title_full Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model
title_fullStr Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model
title_full_unstemmed Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model
title_short Nexrutine® preserves muscle mass similar to exercise in prostate cancer mouse model
title_sort nexrutine r preserves muscle mass similar to exercise in prostate cancer mouse model
topic atrophy
inflammation
natural product
neoplasm of the prostate
proteolysis‐inducing factor
url https://doi.org/10.14814/phy2.14217
work_keys_str_mv AT darpanipatel nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel
AT derekwallace nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel
AT kiraabuchowski nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel
AT paulrivas nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel
AT ambergallegos nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel
AT nicolasmusi nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel
AT addankipratapkumar nexrutinepreservesmusclemasssimilartoexerciseinprostatecancermousemodel